Canonical Allele Identifier: PA204926
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 208814
ClinVar RCV Id: RCV000190842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689632.2:p.Gly133Ala
CA204925
NM_152419.3:c.398G>C